FDA UDI In Commercial Distribution 🇺🇸 United States

Legato®

DI: 04250337115243 · Model: JMPP27025* · Joimax GmbH
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Let the assistant research this device

The Research Assistant compiles product codes, classification, clearances and adverse events for this device — and cites every record.

Free to try · every answer cites its records

Basic Information

Brand Name
Legato®
Primary DI
04250337115243
Version / Model
JMPP27025*
Catalog Number
JMPP27025*
Company Name
Joimax GmbH
Labeler DUNS
344267187
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-02-19
Public Version
3
Public Version Date
2018-07-06
Public Version Status
Update
Public Device Record Key
567635c1-78bc-473d-9dda-fecdc3b972ea

Device Description

Legato® Probe monopolar, Ball Tip, straight

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
GEI Electrosurgical, Cutting & Coagulation & Accessories

GMDN Terms

Code Name
57972 Radio-frequency ablation system

Identifiers

Type ID
Primary 04250337115243
Package 04250337115250

Customer Contacts

Phone
+49721255140

Premarket Submissions

Submission Number Supplement Number
K161378 000